CONSERVE® 38PF1044Recalls & reported problems
Microport Orthopedics Inc. · CONSERVE® CEMENTLESS FEMORAL COMPONENT 44MM · Class 2 · Implant
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI M68438PF10441), received between Feb 21, 2020 and Feb 21, 2020 — classified as 1 injury.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
- Device Dislodged or Dislocated1
Patient problems
- Metal Related Pathology1
- Neurological Deficit/Dysfunction1
- Pain1
- Reaction1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryFeb 21, 2020Device Dislodged or Dislocated; Adverse Event Without Identified Device or Use Problem; Device Dislodged or Dislocated
ALLEGEDLY, ON (B)(6) 2016 SUBJECT BEGAN WITH PAIN, A PSEUDOTUMOR WAS DIAGNOSED THROUGH ULTRASOUND. REVISION WITH FULL IMPLANT REMOVAL OCCURRED ON (B)(6) 2019. ADDITIONAL INFORMATION ON (B)(6) 2018 SUBJECT EXPERIENCED HIP DISLOCATION OF THE RIGHT SIDE AND RECEIVED A REDUCTION ON (B)(6) 2018. SAE # 052-021R-2. ADDITIONAL INFORMATION RECEIVED ON 11/09/2020 FROM CLINICAL: CORRECTING EXPLANT DATE TO (B0(6) 2019 AND PATIENT'S PERSONAL INFORMATION.
Patient problems: Metal Related Pathology; Neurological Deficit/Dysfunction; Pain; Reaction
MAUDE report 9739378 ↗
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- Recap Hip System US157342Biomet Orthopedics, LLC · Prosthesis, hip, femoral, resurfacing1 recall0 reports
- Recap Hip System US157346Biomet Orthopedics, LLC · Prosthesis, hip, femoral, resurfacing1 recall0 reports
- SYNOVO HIP COMPONENTS 01-03-0045Synovo Production · Prosthesis, Hip, Femoral, Resurfacing1 recall0 reports
- Recap Hip System US157356Biomet Orthopedics, LLC · Prosthesis, hip, femoral, resurfacing1 recall0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.